ClinVar Miner

List of variants in gene GRIN2B reported as likely benign

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Gene type:
ClinVar version:
Total variants: 165
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HGVS dbSNP
NM_000834.4(GRIN2B):c.*1074C>T rs201335778
NM_000834.4(GRIN2B):c.*219C>T rs80081965
NM_000834.4(GRIN2B):c.*409T>G rs890
NM_000834.4(GRIN2B):c.*567A>C rs1805503
NM_000834.4(GRIN2B):c.*988A>G rs1805477
NM_000834.4(GRIN2B):c.-12G>A rs201343005
NM_000834.4(GRIN2B):c.-15G>A rs12818068
NM_000834.4(GRIN2B):c.-47G>T
NM_000834.4(GRIN2B):c.1020C>T (p.Ile340=) rs778209882
NM_000834.4(GRIN2B):c.1023T>C (p.Asn341=) rs201228929
NM_000834.4(GRIN2B):c.1038G>A (p.Gly346=) rs753955843
NM_000834.4(GRIN2B):c.1080G>A (p.Pro360=)
NM_000834.4(GRIN2B):c.1080G>T (p.Pro360=) rs201952040
NM_000834.4(GRIN2B):c.1099C>T (p.Leu367=) rs1057522928
NM_000834.4(GRIN2B):c.1125+19A>C rs181390006
NM_000834.4(GRIN2B):c.1126-12A>G rs76777620
NM_000834.4(GRIN2B):c.1176C>A (p.Pro392=) rs1555112397
NM_000834.4(GRIN2B):c.1275G>A (p.Leu425=) rs950679024
NM_000834.4(GRIN2B):c.1338A>G (p.Thr446=) rs141031272
NM_000834.4(GRIN2B):c.1356C>T (p.Tyr452=) rs142935139
NM_000834.4(GRIN2B):c.138C>T (p.Asp46=) rs200527066
NM_000834.4(GRIN2B):c.144G>A (p.Val48=) rs201242152
NM_000834.4(GRIN2B):c.1500+47C>T
NM_000834.4(GRIN2B):c.1500+7G>A rs201094275
NM_000834.4(GRIN2B):c.1501-19C>T rs377609698
NM_000834.4(GRIN2B):c.153G>A (p.Lys51=) rs1057522391
NM_000834.4(GRIN2B):c.1560G>A (p.Ser520=) rs566776310
NM_000834.4(GRIN2B):c.1569C>T (p.Val523=) rs148573953
NM_000834.4(GRIN2B):c.15G>A (p.Ala5=) rs34315573
NM_000834.4(GRIN2B):c.1654+10G>A rs201242368
NM_000834.4(GRIN2B):c.1655-17dup rs768388356
NM_000834.4(GRIN2B):c.1665C>T (p.Ser555=) rs1805482
NM_000834.4(GRIN2B):c.1704C>A (p.Ile568=) rs202102041
NM_000834.4(GRIN2B):c.1704C>T (p.Ile568=) rs202102041
NM_000834.4(GRIN2B):c.174T>C (p.Asp58=) rs1555149549
NM_000834.4(GRIN2B):c.1768G>A (p.Ala590Thr) rs145021339
NM_000834.4(GRIN2B):c.1780+19G>A
NM_000834.4(GRIN2B):c.1806C>T (p.Ile602=) rs1805522
NM_000834.4(GRIN2B):c.1851C>T (p.Ser617=) rs147373250
NM_000834.4(GRIN2B):c.1878C>A (p.Thr626=) rs1555110827
NM_000834.4(GRIN2B):c.1881C>T (p.Thr627=) rs768296067
NM_000834.4(GRIN2B):c.189C>T (p.Ser63=) rs199707487
NM_000834.4(GRIN2B):c.190G>A (p.Val64Met) rs150070901
NM_000834.4(GRIN2B):c.2011-197T>C
NM_000834.4(GRIN2B):c.2011-20_2011-17del rs751965360
NM_000834.4(GRIN2B):c.2017A>C (p.Arg673=) rs149279923
NM_000834.4(GRIN2B):c.2046C>G (p.Arg682=) rs1057522130
NM_000834.4(GRIN2B):c.2172-10del rs761900678
NM_000834.4(GRIN2B):c.2172-20_2172-17del rs765274847
NM_000834.4(GRIN2B):c.2172-4A>G rs367915298
NM_000834.4(GRIN2B):c.2172-6G>A rs201390691
NM_000834.4(GRIN2B):c.2172-8C>T rs751592819
NM_000834.4(GRIN2B):c.2202A>C (p.Ala734=) rs148185805
NM_000834.4(GRIN2B):c.2202A>G (p.Ala734=) rs148185805
NM_000834.4(GRIN2B):c.2247G>A (p.Val749=) rs757990373
NM_000834.4(GRIN2B):c.2250C>G (p.Thr750=) rs752150199
NM_000834.4(GRIN2B):c.228C>T (p.Thr76=) rs77299791
NM_000834.4(GRIN2B):c.2359+16G>A rs781365670
NM_000834.4(GRIN2B):c.2359+16G>C
NM_000834.4(GRIN2B):c.2360-15C>A rs1555103197
NM_000834.4(GRIN2B):c.2481G>A (p.Ala827=) rs189384622
NM_000834.4(GRIN2B):c.2514C>T (p.Cys838=) rs3026160
NM_000834.4(GRIN2B):c.2599-19C>A rs3751258
NM_000834.4(GRIN2B):c.2628G>A (p.Ala876=) rs199710029
NM_000834.4(GRIN2B):c.2664C>T (p.Thr888=) rs1806201
NM_000834.4(GRIN2B):c.2691C>T (p.Asn897=) rs35125534
NM_000834.4(GRIN2B):c.2703G>A (p.Leu901=) rs145005918
NM_000834.4(GRIN2B):c.2715C>T (p.Ala905=) rs568858172
NM_000834.4(GRIN2B):c.2754G>A (p.Pro918=) rs756487785
NM_000834.4(GRIN2B):c.2813G>A (p.Arg938His) rs150445188
NM_000834.4(GRIN2B):c.2826G>A (p.Thr942=) rs140573925
NM_000834.4(GRIN2B):c.2847C>T (p.Tyr949=) rs771565713
NM_000834.4(GRIN2B):c.2856G>A (p.Pro952=)
NM_000834.4(GRIN2B):c.2913G>A (p.Gly971=) rs200696950
NM_000834.4(GRIN2B):c.291G>A (p.Val97=) rs202223470
NM_000834.4(GRIN2B):c.2991C>A (p.Ala997=)
NM_000834.4(GRIN2B):c.3006G>T (p.Gly1002=)
NM_000834.4(GRIN2B):c.3009C>G (p.Leu1003=) rs1460313772
NM_000834.4(GRIN2B):c.3076G>A (p.Gly1026Ser) rs201963596
NM_000834.4(GRIN2B):c.3078C>T (p.Gly1026=) rs1555102406
NM_000834.4(GRIN2B):c.3081C>A (p.Leu1027=)
NM_000834.4(GRIN2B):c.3111C>A (p.Asp1037Glu)
NM_000834.4(GRIN2B):c.3117C>T (p.Tyr1039=) rs147762014
NM_000834.4(GRIN2B):c.3146A>G (p.Tyr1049Cys) rs201866998
NM_000834.4(GRIN2B):c.3174C>T (p.Ser1058=) rs772364390
NM_000834.4(GRIN2B):c.3195C>A (p.Thr1065=) rs879254211
NM_000834.4(GRIN2B):c.3275G>A (p.Arg1092Gln) rs1555102321
NM_000834.4(GRIN2B):c.327C>G (p.Ala109=) rs748395100
NM_000834.4(GRIN2B):c.3285G>A (p.Ser1095=) rs200058641
NM_000834.4(GRIN2B):c.3306T>C (p.Phe1102=) rs763445499
NM_000834.4(GRIN2B):c.3335G>A (p.Arg1112Gln)
NM_000834.4(GRIN2B):c.3339G>A (p.Pro1113=) rs200660626
NM_000834.4(GRIN2B):c.3339G>T (p.Pro1113=) rs200660626
NM_000834.4(GRIN2B):c.336C>T (p.Leu112=) rs1060504845
NM_000834.4(GRIN2B):c.3389G>A (p.Arg1130Gln) rs148625092
NM_000834.4(GRIN2B):c.3456C>A (p.Thr1152=) rs752200554
NM_000834.4(GRIN2B):c.3498C>T (p.Ser1166=) rs45600931
NM_000834.4(GRIN2B):c.3504C>T (p.Ser1168=)
NM_000834.4(GRIN2B):c.3534C>T (p.His1178=) rs1806191
NM_000834.4(GRIN2B):c.3549G>A (p.Thr1183=) rs201568782
NM_000834.4(GRIN2B):c.3552C>T (p.Gly1184=) rs141886903
NM_000834.4(GRIN2B):c.3648C>T (p.Arg1216=) rs201405157
NM_000834.4(GRIN2B):c.3660C>G (p.Ser1220=) rs201983807
NM_000834.4(GRIN2B):c.366C>G (p.Pro122=) rs7301328
NM_000834.4(GRIN2B):c.3690G>A (p.Thr1230=)
NM_000834.4(GRIN2B):c.3714G>T (p.Ala1238=) rs760725802
NM_000834.4(GRIN2B):c.3747C>T (p.Gly1249=) rs138771137
NM_000834.4(GRIN2B):c.3751C>T (p.Leu1251=) rs200186058
NM_000834.4(GRIN2B):c.3797C>T (p.Pro1266Leu) rs201947553
NM_000834.4(GRIN2B):c.3799G>T (p.Ala1267Ser) rs141844705
NM_000834.4(GRIN2B):c.3807A>G (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3807A>T (p.Pro1269=) rs78765966
NM_000834.4(GRIN2B):c.3818C>A (p.Thr1273Lys) rs531747728
NM_000834.4(GRIN2B):c.3819G>A (p.Thr1273=) rs1555101910
NM_000834.4(GRIN2B):c.381C>T (p.His127=) rs200608452
NM_000834.4(GRIN2B):c.3837T>G (p.Thr1279=) rs1806200
NM_000834.4(GRIN2B):c.3945C>T (p.Ala1315=) rs200657400
NM_000834.4(GRIN2B):c.3949C>G (p.Leu1317Val) rs1565453145
NM_000834.4(GRIN2B):c.3957G>A (p.Pro1319=) rs141730031
NM_000834.4(GRIN2B):c.3966A>G (p.Val1322=) rs1555101821
NM_000834.4(GRIN2B):c.3981G>A (p.Lys1327=) rs201670483
NM_000834.4(GRIN2B):c.3993G>A (p.Met1331Ile) rs200035225
NM_000834.4(GRIN2B):c.4014C>T (p.His1338=) rs758288071
NM_000834.4(GRIN2B):c.4101C>T (p.Pro1367=) rs112932810
NM_000834.4(GRIN2B):c.4102G>A (p.Gly1368Ser) rs1043559346
NM_000834.4(GRIN2B):c.4107C>T (p.Gly1369=) rs201732760
NM_000834.4(GRIN2B):c.411+293C>T
NM_000834.4(GRIN2B):c.4113C>T (p.Tyr1371=) rs146792012
NM_000834.4(GRIN2B):c.412-14T>C rs879254251
NM_000834.4(GRIN2B):c.4179C>T (p.Asp1393=) rs199529615
NM_000834.4(GRIN2B):c.4197T>C (p.His1399=) rs1805247
NM_000834.4(GRIN2B):c.4218C>T (p.Phe1406=) rs1805246
NM_000834.4(GRIN2B):c.4235C>A (p.Ala1412Glu) rs1314346300
NM_000834.4(GRIN2B):c.4240G>T (p.Ala1414Ser) rs140744818
NM_000834.4(GRIN2B):c.4241C>T (p.Ala1414Val) rs751107971
NM_000834.4(GRIN2B):c.4269C>T (p.Ala1423=) rs1565452665
NM_000834.4(GRIN2B):c.4287G>A (p.Pro1429=) rs146235271
NM_000834.4(GRIN2B):c.4296G>A (p.Ser1432=) rs755880051
NM_000834.4(GRIN2B):c.4311C>T (p.Ala1437=) rs112265127
NM_000834.4(GRIN2B):c.4322G>A (p.Arg1441His) rs200903876
NM_000834.4(GRIN2B):c.4410T>C (p.Asn1470=) rs199819153
NM_000834.4(GRIN2B):c.4413G>A (p.Gly1471=) rs202051424
NM_000834.4(GRIN2B):c.4416T>G (p.His1472Gln) rs1555101497
NM_000834.4(GRIN2B):c.444A>G (p.Pro148=) rs200658883
NM_000834.4(GRIN2B):c.504C>A (p.Ile168=) rs36031537
NM_000834.4(GRIN2B):c.513C>T (p.Ile171=) rs3026183
NM_000834.4(GRIN2B):c.519C>G (p.Thr173=) rs200357530
NM_000834.4(GRIN2B):c.51C>T (p.Ala17=) rs145404836
NM_000834.4(GRIN2B):c.52G>A (p.Val18Ile) rs201094029
NM_000834.4(GRIN2B):c.540G>A (p.Gln180=) rs1057523105
NM_000834.4(GRIN2B):c.60C>T (p.Ala20=) rs371566007
NM_000834.4(GRIN2B):c.61G>A (p.Val21Met) rs79046967
NM_000834.4(GRIN2B):c.630C>T (p.Asp210=) rs202115787
NM_000834.4(GRIN2B):c.681C>A (p.Ile227=) rs148254591
NM_000834.4(GRIN2B):c.732C>G (p.Ala244=) rs201554036
NM_000834.4(GRIN2B):c.765G>A (p.Thr255=) rs199844735
NM_000834.4(GRIN2B):c.80G>T (p.Arg27Leu) rs200727145
NM_000834.4(GRIN2B):c.812C>A (p.Ala271Glu) rs138098032
NM_000834.4(GRIN2B):c.812C>T (p.Ala271Val) rs138098032
NM_000834.4(GRIN2B):c.834C>A (p.Ile278=) rs199835162
NM_000834.4(GRIN2B):c.870C>T (p.Pro290=) rs1124894
NM_000834.4(GRIN2B):c.96C>A (p.Pro32=) rs374173060
NM_000834.4(GRIN2B):c.975C>T (p.His325=) rs200380868
NM_000834.4(GRIN2B):c.999T>C (p.Asn333=)
NM_000834.4(GRIN2B):c.99C>A (p.Pro33=) rs77738206

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